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Most Online1,568 Jun 29th, 2016
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If you want to use this QR code (Quick Response code) just save the image and paste it where you want. You can even print it and use it that way. Coffee cups, T-Shirts etc would all be good for the QR code.
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Joined: Nov 2009
Posts: 378
Fifth_Degree_AS_Kicker
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Fifth_Degree_AS_Kicker
Joined: Nov 2009
Posts: 378 |
QUOTE: The monthly blood tests were no big deal and I even had 2 beers every Friday when we went out for lunch. QUOTE
Monthly? I had to go every two weeks for over a year!
Mind you, I had a lot more than two beers a week - My drinking pattern never changed. (wish I had smiles here. ;-))
I was told all the scare tactics too, but hey, regular tests that tell you that your drinking isn't affecting your liver - whoohoo. Parteee ;-)
My understanding was that I had to be on MTX for at least a year before I could be considered eligible for biological therapy.(This is in the UK) Blood tests, gaining weight, losing my hair, tinnitus, vertigo, etc, it was all worth it.
I'm on Humira ten months now and it's like I've been given a new lease of life
Everything has side-effects, Rob - even life. It's got a b u g g e r of a one.lol
Take your time, make an informed choice.
Trust me, you will be fine.
Let me know what you decide, I'd be interested to know.
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Joined: Mar 2009
Posts: 185
First_Degree_AS_Kicker
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OP
First_Degree_AS_Kicker
Joined: Mar 2009
Posts: 185 |
Yeah i'm going for blood tests every fortnight too. I'm not a big drinker but good to know that a social one or two a week won't hurt. LOLS Irish you mean i can still partee once in a while?!! Phew!... Glad the Humira is working for you! I'm starting out on low dose 7.5mg and felt no nausea or anything after.. so good start so far. I have a psoriatic skin thing going on too which my doc thinks could be linked to my AS and i'm hoping the MTX might help with that. Anybody else have psoriasis skin issues? Cheers for replies guys. Rob
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Joined: Jul 2001
Posts: 3,334
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Joined: Jul 2001
Posts: 3,334 |
Hi Rob. I have psoriasis and was hoping for any type of noticeable relief after 3 months of MTX, even a little bit. Didn't notice any improvement.
Timo
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Joined: Nov 2009
Posts: 378
Fifth_Degree_AS_Kicker
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Fifth_Degree_AS_Kicker
Joined: Nov 2009
Posts: 378 |
Yup, I have psoriasis too. Mind you, long before I started MTX mine had eased quite a bit. I only have it now on one eye and one ear - yeah, totally attractive. lol (but a hell of a lot better than it was. ;-))
The MTX did nothing for me either.
Would be really interested to know if it works for you, Rob
Partee on!
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Joined: Feb 2009
Posts: 213
Second_Degree_AS_Kicker
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Second_Degree_AS_Kicker
Joined: Feb 2009
Posts: 213 |
Hi Rob, I've been on MTX for 3 years now, initially to treat very stubborn uveitis. It took me about 2 months to get used to it with bad fatigue (started on 15mg/week, max dose to date was 25mg/week) - now it doesn't bother me at all. In those 3 years I first started having SI pain, so MTX clearly wasn't helping that for me (although humira does these days!) - but now that I'm tapering the MTX I think it may have been doing quite a bit for the peripheral joints instead... am definitely experiencing more hand pain now... My blood tests are now 3 months apart. Labs have generally been fine apart from the one taken shortly after I had a bit too much alcohol on a weekend  - although there were also meds in the mix too at the time - liver function normalised again after stopping the other med. Alcohol in moderation should be ok, I was initially advised to not have any day before, day of or day after the MTX dose (which I adhered to a lot more in the first few years than I do now, especially as I take MTX on a Sat) Having said that I did have one cocktail on an MTX day a month or so ago and was seriously ill the next day - won't be doing that again in a hurry!!! But a glass of wine with dinner is fine. Bear in mind though that it's a good idea to drink lots of water whilst on MTX too! Hope it helps you! -Anke
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